# K223901: ApneaRX Pro

- Pathway: 510(k) (Special)
- Applicant: Apnea Sciences Coporation
- Decided: Sep 1, 2023 after 247 days
- Product code: LRK (Device, Anti-Snoring)
- Device class: 2
- Regulation: 21 CFR 872.5570
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K071404 (2007). 13 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K113569: Apnearx, Apnea Science Corporation (2012) Summary page 4.

## Most influential descendants
- K250122: SleepRight Snore Aid (2025), 0 descendants of its own

## Indications for use
The ApneaRx Pro is intended for use on adult patients 18 years of age or older as an aid for the reduction of mild to moderate obstructive sleep apnea (OSA), and/or snoring.

Source page: https://510kreport.com/device/K223901
Methodology: https://510kreport.com/methodology